Beta Oxidation

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Fatty acid oxidation

by
Dr.Jothi Malar MD,DNB

The purpose of oxidation of Fatty acid


is to generate energy

Types of Fatty acid oxidation:

1. - oxidation
2. Peroxisomal oxidation
3. - oxidation
4. - oxidation

Fatty acid oxidation


Site : all tissues , prominent in liver and skeletal
muscle.
Intracellular location: mitochondria.
Substrate: fatty acids.
Product: acetyl CoA, NADH, FADH2

Release of FA from
adipose tissue

Steps in fatty acid oxidation

Activation of fatty acids


Transport of fatty acids across mitochondrial
membranes into mitochondrial matrix
Beta oxidation of fatty acids.

Activation of fatty acids


FA are activated to fatty acyl CoA by acyl CoA synthase
(thiokinase) present in the cytoplasm, outer mitochondrial
membrane or ER.
By activation the relative stability of -C-C- bond in a FA is
overcome, which allows stepwise oxidation.

There are different isoforms of Fatty acyl CoA synthase


specific for different kind of FAs.
Fatty acid + ATP + CoA

--->

Acyl-CoA + PPi + AMP

Carnitine as a Carrier

Carnitine carries fatty acyl groups across the inner


mitochondrial membrane
Mitochondrial inner membrane is impermeable to bulky
polar molecules like CoA.
Hence acyl group from cytosol is carried into mitochondrial
matrix by carnitine- carnitine shuttle.
Short chain fatty acids are carried directly into the
mitochondrial matrix
Long-chain and medium chain FAs are converted to acyl
carnitines and are then transported in to the mitochondria.
Acyl-CoA are reformed inside the mitochondria

Carnitine
Synthesized from
lysine & methionine in
liver and kidney

Carnitine shuttle

Carnitine deficiency
Causes : primary - decreased production as in neonates.
Secondary:

Renal leakage
Hemodialysis
Valproic acid- inhibits renal reabsorption
Organic acidurias

Organs involved:

Heart-cardiomyopathy, arrhythmias, sudden death.


Liver- hepatomegaly
Muscle myopathy-mild cramps to severe muscle weakness.
CNS: encephalopathy, hypoketotic hypoglycemia

Effects are due to decreased FA oxidation leading to


FA accumulation. Utilization of glucose and
decreased gluconeogenesis leads to hypoglycemia.
Treatment : carnitine

Beta Oxidation
Oxidation of fatty acids to acetyl CoA

COOH

In this process the carbon is oxidised via a ketone intermediate to a thioester

-Oxidation of Fatty Acids


A Repeated Sequence of 4 Reactions
Strategy: create a carbonyl group on the -C
First 3 reactions do that; fourth cleaves the "-keto ester
Products: an acetyl-CoA and a fatty acid two carbons
shorter

Beta-oxidation
Four enzymatic reactions:
1.Dehydrogenation between alpha and beta
carbons(C2 and C3) in a FAD-linked reaction.
2.Hydration of the double by enoyl CoA hydratase.
3.A second dehydrogenation in a NAD-linked reaction.
4.Thiolytic cleavage of the thioester by beta-ketoacyl
CoA thiolase.
This sequence of reactions repeated until the fatty acyl
chain is completely degraded to acetyl CoA.\

Acyl-CoA Dehydrogenase

Oxidation of the C-C bond


There are three fatty acyl CoA dehydrogenases specific
for a different acyl chain length. Different enzymes are
involved indifferent stages of beta oxidation.
Long chain acyl CoA dehydrogenase(LCAD) acts on
chains greater C12.
MCAD acts on C6 to C12.
SCAD acts on C4 to C6.
MCAD deficiency is one of the most common error of
metabolism resulting in sudden infant death syndrome.
Enzyme is inhibited by a metabolite of hypoglycin (from
akee fruit)

Beta oxidation of fatty acids

Beta oxidation of fatty acids

Beta oxidation of fatty acids

Complete Beta Oxidation of Palmitoyl CoA

7 Cycles

8 CH3COSCoA + 7 FADH2 + 7 NADH + 7 H

For example for a 16 carbon fatty acid, PalmitylCoA, it will take 7 cycle of -oxidation to generate 8
acetyl-CoA.

Thus there will be production of 7 FADH2, 7 NADH


molecules during the -oxidation cycles.

Oxidation of 8 acetyl-CoA in TCA cycle will


produce 8 ATPs, 8 FADH2, 24 NADH

Energy yield from palmitic acid


From palmitoyl CoA to acetyl CoA:
Acyl CoA dehydrogenase 7 FADH2
Beta-OH dehydrogenase 7 NADH
From 8 acetyl CoA
Total energy yield
ATP are used for activation of FA
Hence net gain of ATP

ATP
14
21
96
131
-2
129

Though it produces more energy, it does not directly


produce ATP during the oxidation steps(no substrate
level phosphorylation)
-Oxidation yields Acetyl CoA,NADH & FADH,requiring
TCA cycle and Respiratory chain for further metabolism
TCA cycle and Respiratory chain requires O2
So Fatty acid cannot be used as an energy source in the
absence of O2

Regulation of fatty acid oxidation


1.

Factors regulating mobilization of FFA from adipose


tissue: liver has a large capacity to take as much as
30 - 50% of FFA from plasma both in fed and fasted
state. But the release of FFA from adipose tissue is
more in starvation(hypoglycemia inhibits Insulin
release).

2.

Inhibitory effect of malonyl CoA on CAT-1.


Fed state: insulin activates Acetyl CoA carboxylase to
form malonyl CoA. Malonyl CoA inhibits CAT-1
resulting in decreased beta oxidation.
starvation state: increase in FFA, inhibition of ACC
activity, decreased malonylCoA Concentration leading
to increased fatty acid oxidation. Reinforced by
insulin:glucagon ratio.

CPT-1(carnitine palmitoyl transferase-1) or CAT1(carnitine acyl transferase-1) is associated with the


inner leaflet of the outer mitochondrial membrane.
CPT-1 reaction is the rate limiting enzyme. It is
allosterically inhibited by malonyl CoA. Malonyl CoA
concentration is high during the fed state.

Hormonal Regulation of Fatty Acid Synthesis and Breakdown


Stimulates Glucagon

Insulin

Phosphodiesterase

Adenylyl cyclase

ATP

Stimulates

cAMP
Activates Protein Kinase
Inactivates Acetyl CoA carboxylase
by phosphorylation
Activates lipase

Inhibition of fatty acid synthesis


and increase of lipolysis and
release of FFA

AMP
Inactivates lipase
Activate acetyl CoA
carboxylase

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